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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25044Generated: October 25, 2026

Cyanuric chloride → 4-[[4-Chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrile

https://huagongshe.com/reaction/25044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant4-AminobenzonitrileHCID 13396—
Reactant1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
ReactantMagnesiumHCID 5462224—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
SolventDiisopropylethylamineHCID 81531—
Product4-[[4-Chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrileHCID 486423104.2%

Reaction Steps

A solution of 2-(bromomethyl)-1,3-dichlorobenzene (about 10% of 0.383 mol) in diethylether (240 ml) was added to magnesium (0.383 mol) in diethylether (240 ml) under argon. Once the reaction started, the remainder of 2-(bromomethyl)-1,3-dichlorobenzene in diethylether was added. The solution was stirred at RT for 2.5 hours and then added via canula to a solution of 2,4,6-trichloro-1,3,5-triazine (0.319 mol) in benzene (480 ml) while keeping the temperature below 15° C. The reaction mixture was stirred for one hour in an ice bath, then for 2 hours at RT. A solution of 4-amino-benzonitrile (0.351 mol) in N,N-diisopropylethylamine (61.0 ml) and 1,4-dioxane (500 ml) was added and the reaction mixture was stirred at RT for 40 hours. The solvent was evaporated. Water and ethylacetate were added. The solution was stirred, then the solid was filtered off, washed with ethylacetate and water, yielding 129.9 g of 4-[[4-chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-amino]benzonitrile (intermediate 27; mp. 243-244° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858609B2
Source datasetuspto-grants-2005_02
ORD IDord-a24fe50e94d9483d807f5b9ce3c92b2c
Source noteuspto-grants-2005_02